Carbohydrates: structure and Function

1. Carbohydrates: structure and Function By Dr. Sumbul Fatma

2. Objectives To understand: • The structure of carbohydrates of physiological significance • The main role of carbohydrates in providing and storing of energy • The structure and function of glycosaminoglycans

3. OVERVIEW Carbohydrates: The most abundant organic molecules in nature The empiric formula is (CH2O)n, “hydrates of carbon” Carbohydrates: provide important part of energy in diet Act as the storage form of energy in the body are structural component of cell membranes

4. OVERVIEW CONT’D • Many diseases associated with disorders of carbohydrate metabolism including: Diabetes mellitus Galactosemia Glycogen storage diseases Lactose intolerance

5. CLASSIFICATION • Monosaccharides: Simple sugar • Disaccharides: 2 monosaccharide units • Oligosaccharides: 3-10 monosaccharide units • Polysaccharides: more than 10 sugar units Homopolysaccharides & heteropolysaccharides

6. Monosaccharides Further classified based on: 1. No. of carbon atoms 2. Functional sugar group: Aldehyde group – aldoses Keto group – ketoses

7. Monosaccharides CONT’D

8. Isomerism • Isomers Compounds having samechemical formula but different structural formula

9. Aldo-Keto Isomers Example: Glucose (Aldose) and Fructose (Ketose)

10. Epimers • Epimers CHO dimers that differ in configuration around only one specific carbon atom -Glucose and galactose, C4 -Glucose and Mannose, C2 Galactose and mannose are not epimers

11. Enantiomers (D- and L-Forms) Structures that are mirror images of each other and are designated as D- and L- sugars based on the position of –OH grp on the asymmetric carbon farthest from the carbonyl carbon Majority of sugars in humans are D-sugars

12. α- and β-Forms • Cyclization of Monosaccharides Monosaccharides with 5 or more carbon are predominantly found in the ring form • The aldehyde or ketone grp reacts with the –OH grp on the same sugar • Cyclization creates an anomericcarbon (former carbonyl carbon) generating the α and β configurations

13. Mutarotation In solution, the cyclic α and β anomers of a sugar are in equilibrium with each other, and can be interconverted spontaneously Fischer Projection Haworth Projection Fischer Projection

14. Sugar Isomers • Aldo-keto • Epimers • D- and L-Forms • α- and β-anomers

15. Disaccharides • Joining of 2 monosaccharides by O-glycosidic bond: Maltose (α-1, 4)= glucose + glucose Sucrose (α-1,2) = glucose + fructose Lactose (β-1,4) = glucose + galactose

16. Disaccharides CONT’D Lactose

17. Polysaccharides • Homopolysaccharides: Branched: Glycogen and starch (α-glycosidic polymer) Unbranched: Cellulose (β-glycosidic polymer) • Heteropolysaccharides: e.g., glycosaminoglycans (GAGs)

18. Reducing Sugars • If the O on the anomeric C of a sugar is not attached to any other structure (Free),that sugar can act as a reducing agent • Reducing sugars reduce chromogenic agents like Benedict’s reagent or Fehling’s solution to give a colored precipitate • Urine is tested for the presence of reducing sugars using these colorimetric tests

19. Reducing Sugars CONT’D • Examples: Monosaccharides Maltose and Lactose Sucrose is non-reducing, Why?

20. Complex Carbohydrates • Carbohydrates attached to non-carbohydrate structures by glycosidic bonds (O- or N-type) e.g., 1. Purine and pyrimidine bases in nucleic acids 2. Bilirubin 3. Proteins in glycoproteins and proteoglycans 4. Lipids found in glycolipids

21. Glycosidic Bonds • N-Glycosidic • O-Glycosidic

22. Glycosaminoglycans (GAGs) • Glycosaminoglycans (GAGs) are large complexes of negativelycharged heteropolysaccharide chains • are associated with a small amount of protein, forming proteoglycans, which consist of over 95 percent carbohydrate • bind with large amounts of water, producing the gel-like matrix that forms body's ground substance • The viscous, lubricating properties of mucous secretions also result from GAGs, which led to the original naming of these compounds as mucopolysaccharides

23. Glycosaminoglycans (GAGs) • GAGs are linear polymers of repeating disaccharide units [acidic sugar-amino sugar]n • The amino sugar (usually sulfated) is either D-glucosamine or D-galactosamine • The acidic sugar is either D-glucuronic acid or L-iduronic acid • GAGs are strongly negatively-charged: carboxyl groups of acidic sugars Sulfate groups

24. Resilience of GAGs Relationship between glycosaminoglycan structure and function • Because of negative charges, the GAG chains tend to be extended in solution and repel each other and when brought together, they "slip" past each other This produces the "slippery" consistency of mucous secretions and synovial fluid • When a solution of GAGs is compressed, the water is "squeezed out" and the GAGs are forced to occupy a smaller volume. When the compression is released, the GAGs spring back to their original, hydrated volume because of the repulsion of their negative charges This property contributes to the resilience of synovial fluid and the vitreous humor of the eye

25. Members of GAGs Examples of GAGs are: • Chondroitin sulfates: Most abundant GAG • Keratan sulfates: Most heterogeneous GAGs • Hyaluronic acid: Compared to other GAGs, it is unsulfated and not covalently attached to protein • Heparin: Unlike other GAGs, Unlike other GAGs that are extracellular, heparin is intracellular and serves as an anticoagulant

26. Take home Message Structure and function of carbohydrates • Mono-, Di-, and Poly-saccharides • Sugar Isomers: Aldo-keto, epimers, D- and L-, α- and β-anomers • Complex carbohydrates: e.g., Glycosaminoglycans and proteoglycans • Structure and function of GAGs • Examples of GAGs: chondroitin sulfate, keratin sulfate, hyaluronic acid and heparin

27. Reference • Lippincott’s Illustrated reviews- Biochemistry, 4th Edition